Regulatory Affairs Manager

Role- Senior Regulatory Affairs Specialist Location - Hampshire - Home working Some travel to site every few months for collaborative projects Supports Regulatory Affairs Project core team members on development teams, providing regulatory guidance, and project regulatory assessments. Liaises with internal functions such as Manufacturing, R&D,...

Role- Senior Regulatory Affairs Specialist Location - Hampshire - Home working Some travel to site every few months for collaborative projects Scope: Supports Regulatory Affairs Project core team members on development teams, providing regulatory guidance, and project regulatory assessments. Liaises with internal functions such as Manufacturing, R&D,...

Job Description Our client, an independent pharmaceutical company who manufacture and specialising in generics, have an opportunity for an experienced EU/ UK Regulatory team leader to join their team in Hampshire. As Regulatory Affairs manager, you will: Leading a small team, handling the regulatory activity across a large portfolio of medicine and...

We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid...

Head of Regulatory Affairs and Pharmacovigilance We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in...

Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely. As a Regulatory Affairs...

We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid...

We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid...

MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a UK based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the UK Responsibilites: Manage the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products...

We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area. As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations. This will be a hybrid...

We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product information modifications. ...

About Our Client Our client is a globally recognised leader within the medical devices space. With a strong presence in over 100 countries, they are renowned for producing cutting-edge research and innovative solutions that have greatly impacted patients lives around the globe. Job Description Oversee and ensure all regulatory affairs are compliant...

SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic...

Our client is a fast growing medical devices consultancy, specialising in regulatory compliance, patents, clinical investigation and market entry. Ensure compliance with all relevant regulatory standards and guidelines within the healthcare industry. Develop and implement Regulatory Affairs and Quality Assurance strategies. Provide guidance and...

In this company, you will play a key role in ensuring regulatory compliance for our client's Class III Orthopaedic products. The successful candidate will have a strong background working with Notified Bodies, technical file remediation and creation, risk management, and global product submissions. Collaborate with Notified Bodies to ensure compliance...

In this company, you will play a key role in ensuring regulatory compliance for our client's Class III Orthopaedic products. The successful candidate will have a strong background working with Notified Bodies, technical file remediation and creation, risk management, and global product submissions. Collaborate with Notified Bodies to ensure compliance...

Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely. As a Regulatory Affairs...

Job Description Regulatory Affairs Manager CMC Duration: 6 month Contract Inside IR35 Location: Uxbridge, 3 days on-site per week Hourly Rate: £40-£55 per hour dependent on experience. This role focuses on the critical aspect of Chemistry, Manufacturing, and Controls (CMC) within regulatory affairs. Responsibilities include: Leading global regulatory...

RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2...

RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past 2...